Department of Clinical Oncology, K1-P, Leiden University Medical Center, Albinusdreef 2, 2333 Leiden, The Netherlands.
Cancer Immunol Immunother. 2012 Jan;61(1):119-25. doi: 10.1007/s00262-011-1160-x. Epub 2011 Nov 25.
Deficiencies in MHC class I antigen presentation are a common feature of tumors and allows escape from cytotoxic T lymphocyte (CTL)-mediated killing. It is crucial to take this capacity of tumors into account for the development of T-cell-based immunotherapy, as it may strongly impair their effectiveness. A variety of escape mechanisms has been described thus far, but progress in counteracting them is poor. Here we review a novel strategy to target malignancies with defects in the antigenic processing machinery (APM). The concept is based on a unique category of CD8+ T-cell epitopes that is associated with impaired peptide processing, which we named TEIPP. We characterized this alternative peptide repertoire emerging in MHC-I on tumors lacking classical antigen processing due to defects in the peptide transporter TAP (transporter associated with peptide processing). These TEIPPs exemplify interesting parallels with the folktale figure Cinderella: they are oppressed and neglected by a stepmother (like functional TAP prevents TEIPP presentation), until the suppression is released and Cinderella/TEIPP achieves unexpected recognition. TEIPP-specific CTLs and their cognate peptide-epitopes provide a new strategy to counteract immune evasion by APM defects and bear potential to targeting escape variants observed in a wide range of cancers.
MHC I 类抗原呈递的缺陷是肿瘤的一个常见特征,这使得肿瘤能够逃避细胞毒性 T 淋巴细胞 (CTL)介导的杀伤。在开发基于 T 细胞的免疫疗法时,必须考虑到肿瘤的这种能力,因为这可能会严重削弱其疗效。迄今为止,已经描述了多种逃逸机制,但对抗这些机制的进展却很差。在这里,我们回顾了一种针对抗原加工机制 (APM) 缺陷的恶性肿瘤的新策略。该概念基于与肽加工受损相关的独特的一类 CD8+ T 细胞表位,我们将其命名为 TEIPP。我们对由于肽转运蛋白 TAP(肽加工相关转运蛋白)缺陷而导致经典抗原加工缺失的 MHC-I 上出现的这种替代肽库进行了表征。这些 TEIPPs 与民间故事灰姑娘有有趣的相似之处:它们受到继母(功能性 TAP 阻止 TEIPP 呈递)的压迫和忽视,直到抑制作用解除,灰姑娘/TEIPP 获得意想不到的识别。TEIPP 特异性 CTL 和它们的同源肽表位为对抗 APM 缺陷的免疫逃逸提供了一种新策略,并有可能针对广泛存在于各种癌症中的逃逸变体。